Portal vein embolisation with application of haematopoietic stem cells in patients with primarily or non-resectable colorectal liver metastases
Jazyk angličtina Země Řecko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25503161
PII: 34/12/7279
Knihovny.cz E-zdroje
- Klíčová slova
- Colorectal liver metastases, future liver remnant volume, haematopoietic stem cells, portal vein embolisation,
- MeSH
- hematopoetické kmenové buňky MeSH
- hepatektomie MeSH
- játra krevní zásobení patologie chirurgie MeSH
- kolorektální nádory mortalita patologie terapie MeSH
- leukaferéza MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory jater mortalita sekundární terapie MeSH
- přežití bez známek nemoci MeSH
- regenerace jater * MeSH
- senioři MeSH
- terapeutická embolizace * MeSH
- transplantace hematopoetických kmenových buněk metody MeSH
- vena portae MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
BACKGROUND: Insufficient future liver remnant volume (FLRV) is the main cause of low resectability of liver metastases from colorectal cancer (CLMs). One option for enhancing FLVR growth is the use of portal vein embolisation (PVE) with the application of autologous haematopoietic stem cells (HSCs). PATIENTS AND METHODS: PVE with the application of HSCs was used in 11 patients (group 1) with primarily non-resectable CLMs due to insufficient FLRV without signs of extrahepatic metastases. The control group (group 2) consisted of 14 patients in whom only PVE was performed. We evaluated the product quality, FLRV growth, CLM volume, median survival and progression-free survival (PFS). RESULTS: Product quality was achieved in all collections. In all group-I patients, sufficient FLRV growth occurred within three weeks. In the first and second weeks, FLRV increased optimally in most patients (p<0.006). In 13 out of the 14 group-2 patients, optimum FLVR growth was observed within three weeks following PVE (p<0.002). More rapid FLVR growth was observed in group 1 patients (p<0.01). CLM volume was significantly increased in both the group-2 (p<0.0005) and group-1 (p<0.008) patients at the time of liver resection. There was no significant difference in the growth of the CLM volume between the groups (p<0.18). The median survival was 7.3 and 6.8 months for group 1 and 2 patients, respectively, and the two-year PFS was 28% and 22% (p<0.18), respectively. CONCLUSION: PVE with HSC application is a promising method for effectively stimulating FLRV growth in patients with primarily non-resectable CLMs.
Department of Hematooncology University Hospital Faculty of Medicine in Pilsen Pilsen Czech Republic
Department of Surgery University Hospital Faculty of Medicine in Pilsen Pilsen Czech Republic
Laboratory of Immunoanalysis University Hospital Faculty of Medicine in Pilsen Pilsen Czech Republic
Radiodiagnostic Clinic University Hospital Faculty of Medicine in Pilsen Pilsen Czech Republic